Results 171 to 180 of about 15,419 (219)
Natural history of simple and complex cysts in autosomal dominant polycystic kidney disease on MRI. [PDF]
Hu Z, Li C, Blumenfeld JD, Prince MR.
europepmc +1 more source
Long-Read Sequencing of CAH and ADPKD Provides Novel Insights Into the Genetic Diagnosis of Male Infertility. [PDF]
Li X +6 more
europepmc +1 more source
Octreotide long-acting release in the treatment of autosomal dominant polycystic kidney disease: a meta-analysis. [PDF]
Jin M, Shi P, Yu Y.
europepmc +1 more source
Prenatal Diagnosis and Postnatal Outcomes of Fetal ADPKD: A Single-Center Retrospective Cohort Study. [PDF]
Kim S +6 more
europepmc +1 more source
PERADIGM: Phenotype embedding similarity-based rare disease gene mapping. [PDF]
Zheng W +6 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
A novel ADPKD model using kidney organoids derived from disease-specific human iPSCs
Biochemical and Biophysical Research Communications, 2020Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disorder which manifests progressive renal cyst formation and leads to end-stage kidney disease.
Keisuke Okita +2 more
exaly +2 more sources
Advanced Healthcare Materials, 2019
There is currently no cure for gene mutation‐caused autosomal dominant polycystic kidney disease (ADPKD). Over half of patients with ADPKD eventually develop kidney failure, requiring dialysis or kidney transplantation.
Si-Tse Jiang, Yi-Che Lee, Yuan-Yow Chiou
exaly +2 more sources
There is currently no cure for gene mutation‐caused autosomal dominant polycystic kidney disease (ADPKD). Over half of patients with ADPKD eventually develop kidney failure, requiring dialysis or kidney transplantation.
Si-Tse Jiang, Yi-Che Lee, Yuan-Yow Chiou
exaly +2 more sources
New treatment paradigms for ADPKD: moving towards precision medicine
Nature Reviews Nephrology, 2017Matthew Bruce Lanktree
exaly +2 more sources

